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Glucose Paracélsia

Active Ingredient:
Glucose
Origin:
EU

Glucose Paracélsia (Glucose)

Glucose Paracélsia is an intravenous solution that contains glucose as its sole active ingredient. The product is supplied in a sterile liquid form for parenteral administration, with the specific concentration not disclosed publicly. It is marketed in the European Union and is available by prescription only. As an excipient‑type drug, it is used primarily to provide an immediate source of carbohydrate energy and to support intravascular volume when infused.

Manufacturer / TM Owner

Laboratórios Basi – Indústria Farmacêutica, S.A.

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Indications & Clinical Uses

Glucose Paracélsia is indicated for several clinical situations where rapid carbohydrate supplementation or fluid replacement is required.

  • Treatment of hypoglycemia in patients unable to take oral glucose.
  • Intravenous fluid replacement for patients with low intravascular volume.
  • Component of parenteral nutrition regimens to meet caloric needs.
  • Support during surgical procedures to maintain blood glucose levels.
  • Adjunct in emergency care when immediate energy source is needed.
  • Use in pediatric patients for rapid correction of low blood glucose under medical supervision.
  • Utilized in critical care settings to assist with hemodynamic stabilization when combined with other electrolytes.

Side Effects

Glucose Paracélsia may be associated with a range of adverse effects, most of which are related to the intravenous administration of a carbohydrate solution.

Common

  • Transient hyperglycemia when administered in excess.
  • Local irritation or pain at the infusion site.
  • Mild electrolyte shifts, such as slight sodium or potassium changes.
  • Nausea or vomiting if the solution is infused rapidly.
  • Headache related to rapid changes in blood glucose concentration.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Volume overload causing pulmonary edema in susceptible patients.
  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Hyperosmolar hyperglycemic state in patients with impaired insulin response.
  • Metabolic acidosis secondary to excessive glucose metabolism.

Precautions & Warnings

When prescribing Glucose Paracélsia, clinicians should consider several precautionary measures to minimize risk and ensure appropriate use.

  • Assess baseline blood glucose and adjust infusion rate to avoid hyperglycemia.
  • Evaluate fluid status and cardiac function to prevent volume overload.
  • Use caution in patients with renal impairment due to altered glucose handling.
  • Monitor electrolytes, especially sodium and potassium, during and after infusion.
  • Avoid rapid bolus administration; prefer controlled infusion to reduce osmotic effects.
  • Consider pregnancy and lactation status; data are limited, so use only if clearly indicated.

Avoid Interactions

Glucose Paracélsia can interact with other intravenous therapies; awareness of potential interactions helps maintain patient safety.

Avoid

  • Co‑administration with high‑dose insulin infusions without glucose monitoring, which may precipitate severe hypoglycemia.
  • Simultaneous infusion of hypertonic saline solutions that could exacerbate hypernatremia.

Use with caution

  • Concurrent use with other carbohydrate‑containing fluids; adjust total glucose load to prevent hyperglycemia.
  • Administration alongside diuretics that affect fluid balance; monitor volume status closely.
  • Use with vasopressors that may alter peripheral perfusion; observe infusion site for signs of irritation.
  • Interaction with potassium‑sparing agents may increase serum potassium; check levels regularly.

Frequently Asked Questions

Glucose Paracélsia is primarily used to treat hypoglycemia, provide fluid replacement, and serve as a carbohydrate source in parenteral nutrition regimens.

The product is supplied as a sterile intravenous solution and is administered directly into a vein under medical supervision.

Yes, it may be used in pediatric patients for rapid correction of low blood glucose, but dosing and monitoring must be performed by qualified healthcare professionals.

Blood glucose levels, fluid balance, electrolytes, and signs of volume overload should be regularly monitored throughout the infusion.

Common side effects include transient hyperglycemia, local infusion site irritation, mild electrolyte shifts, nausea, vomiting, and headache.

It should be avoided in patients receiving high‑dose insulin infusions without appropriate glucose monitoring and when co‑infused with hypertonic saline that could cause hypernatremia.

Safety data in pregnancy are limited; it should only be used when clearly indicated and after evaluating potential risks and benefits.

When infused, the glucose solution adds osmotic load and fluid volume to the bloodstream, helping to expand intravascular volume in hypovolemic patients.

Serious reactions may include severe hyperglycemia with osmotic diuresis, volume overload leading to pulmonary edema, allergic reactions such as anaphylaxis, hyperosmolar hyperglycemic state, and metabolic acidosis.

It can be combined with other IV fluids, but total glucose load and electrolyte composition should be carefully calculated to avoid hyperglycemia or electrolyte imbalance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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